PL299376A1 - Method of making solid dosage units of controllable release - Google Patents

Method of making solid dosage units of controllable release

Info

Publication number
PL299376A1
PL299376A1 PL91299376A PL29937691A PL299376A1 PL 299376 A1 PL299376 A1 PL 299376A1 PL 91299376 A PL91299376 A PL 91299376A PL 29937691 A PL29937691 A PL 29937691A PL 299376 A1 PL299376 A1 PL 299376A1
Authority
PL
Poland
Prior art keywords
dosage units
solid dosage
making solid
controllable release
granulation
Prior art date
Application number
PL91299376A
Other versions
PL168605B1 (en
Inventor
Per Johan Gunnar Lundberg
Original Assignee
Astra Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Astra Ab filed Critical Astra Ab
Publication of PL299376A1 publication Critical patent/PL299376A1/en
Publication of PL168605B1 publication Critical patent/PL168605B1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1652Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1682Processes
    • A61K9/1694Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient

Landscapes

  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
  • Ultra Sonic Daignosis Equipment (AREA)
  • Control Of Vending Devices And Auxiliary Devices For Vending Devices (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Abstract

A method for the manufacture of oral controlled release dosage units containing hydroxypropyl methylcellulose wherein the aqueous granulation is performed in the presence of one or more solutes, which inhibit gel formation during the granulation but allows the formation of a gel when administered orally. Also the new dosage units prepared according to the invention are included.
PL91299376A 1990-12-07 1991-12-03 Method of making solid dosage units of controllable release PL168605B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE9003904A SE9003904D0 (en) 1990-12-07 1990-12-07 METHOD FOR THE MANUFACTURE OF A PHARMACEUTICAL DOSAGE FORM
PCT/SE1991/000813 WO1992010169A1 (en) 1990-12-07 1991-12-03 Method for the manufacture of a controlled release solid unit dosage form

Publications (2)

Publication Number Publication Date
PL299376A1 true PL299376A1 (en) 1994-03-07
PL168605B1 PL168605B1 (en) 1996-03-29

Family

ID=20381123

Family Applications (1)

Application Number Title Priority Date Filing Date
PL91299376A PL168605B1 (en) 1990-12-07 1991-12-03 Method of making solid dosage units of controllable release

Country Status (20)

Country Link
US (1) US5419918A (en)
EP (1) EP0560822B1 (en)
JP (1) JP3239319B2 (en)
AT (1) ATE130188T1 (en)
AU (1) AU659114B2 (en)
CA (1) CA2097175A1 (en)
DE (1) DE69114721T2 (en)
DK (1) DK0560822T3 (en)
ES (1) ES2079689T3 (en)
FI (1) FI932552A0 (en)
GR (1) GR3018685T3 (en)
HU (1) HUT64212A (en)
IE (1) IE914229A1 (en)
IS (1) IS3789A7 (en)
NO (1) NO932054L (en)
PL (1) PL168605B1 (en)
PT (1) PT99721A (en)
SE (1) SE9003904D0 (en)
WO (1) WO1992010169A1 (en)
YU (1) YU182091A (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3598049B2 (en) * 1992-09-18 2004-12-08 山之内製薬株式会社 Hydrogel sustained release formulation
DK0661045T3 (en) * 1992-09-18 2002-10-28 Yamanouchi Pharma Co Ltd Delayed release hydrogel preparation
ES2059260B1 (en) * 1992-10-06 1995-04-16 Espanola Prod Quimicos PROCEDURE FOR THE PREPARATION OF TABLETS CONTAINING DICLOFENACO; DISPERSIBLE IN WATER.
US5393765A (en) * 1993-12-13 1995-02-28 Hoffmann-La Roche Inc. Pharmaceutical compositions with constant erosion volume for zero order controlled release
US5948437A (en) * 1996-05-23 1999-09-07 Zeneca Limited Pharmaceutical compositions using thiazepine
JP2000034224A (en) * 1998-05-11 2000-02-02 Freunt Ind Co Ltd Sustained-release tablet, additive composition for the tablet, and their production
US6368625B1 (en) 1998-08-12 2002-04-09 Cima Labs Inc. Orally disintegrable tablet forming a viscous slurry
US6214381B1 (en) 1998-09-08 2001-04-10 Effcon, Inc. Methazolamide composition and method of use
WO2003011256A1 (en) * 2001-07-30 2003-02-13 Sun Pharmaceutical Industries Limited Oral controlled release pharmaceutical composition of a prokinetic agent
US20030068375A1 (en) 2001-08-06 2003-04-10 Curtis Wright Pharmaceutical formulation containing gelling agent
US20040185093A1 (en) * 2003-03-18 2004-09-23 Szymczak Christopher E. Compositions containing sucralose
US20060062811A1 (en) * 2004-09-21 2006-03-23 Szymczak Christopher E Medicinal cooling emulsions
SA07280459B1 (en) 2006-08-25 2011-07-20 بيورديو فارما إل. بي. Tamper Resistant Oral Pharmaceutical Dosage Forms Comprising an Opioid Analgesic
WO2014170755A2 (en) * 2013-04-16 2014-10-23 Murray And Poole Enterprises Limited Sustained-release formulations of colchicine and methods of using same
US9980946B1 (en) 2017-01-25 2018-05-29 Effcon Laboratories, Inc. Extended release methazolamide formulation
JP7426685B2 (en) * 2018-06-14 2024-02-02 株式会社東洋新薬 tablet

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4369172A (en) * 1981-12-18 1983-01-18 Forest Laboratories Inc. Prolonged release therapeutic compositions based on hydroxypropylmethylcellulose
FR2525474A1 (en) * 1982-04-26 1983-10-28 Roussel Uclaf NEW ORAL PHARMACEUTICAL FORM OF CLOMETACIN
US4559384A (en) * 1983-12-20 1985-12-17 Toyo Soda Manufacturing Co., Ltd. Process for preventing agglomeration of powders by using triethylenediamine polymers
US4795327A (en) * 1984-03-26 1989-01-03 Forest Laboratories, Inc. Controlled release solid drug dosage forms based on mixtures of water soluble nonionic cellulose ethers and anionic surfactants
EP0294493A4 (en) * 1986-12-25 1989-07-24 Teysan Pharmaceuticals Co Ltd Slowly soluble granule and persistently effective composite granule prepared therefrom.
US4786503A (en) * 1987-04-06 1988-11-22 Alza Corporation Dosage form comprising parallel lamine
US4971805A (en) * 1987-12-23 1990-11-20 Teysan Pharmaceuticals Co., Ltd. Slow-releasing granules and long acting mixed granules comprising the same
US5024842A (en) * 1988-04-28 1991-06-18 Alza Corporation Annealed coats
CA2002492A1 (en) * 1988-11-11 1990-05-11 Sandra T. A. Malkowska Pharmaceutical ion exchange resin composition

Also Published As

Publication number Publication date
ATE130188T1 (en) 1995-12-15
JPH06503310A (en) 1994-04-14
CA2097175A1 (en) 1992-06-08
IE914229A1 (en) 1992-06-17
PT99721A (en) 1993-04-30
JP3239319B2 (en) 2001-12-17
AU8930991A (en) 1992-07-08
EP0560822A1 (en) 1993-09-22
HUT64212A (en) 1993-12-28
DK0560822T3 (en) 1996-03-11
WO1992010169A1 (en) 1992-06-25
YU182091A (en) 1994-04-05
SE9003904D0 (en) 1990-12-07
FI932552A (en) 1993-06-04
DE69114721T2 (en) 1996-04-18
PL168605B1 (en) 1996-03-29
IS3789A7 (en) 1992-06-08
US5419918A (en) 1995-05-30
EP0560822B1 (en) 1995-11-15
NO932054D0 (en) 1993-06-04
NO932054L (en) 1993-06-04
ES2079689T3 (en) 1996-01-16
DE69114721D1 (en) 1995-12-21
AU659114B2 (en) 1995-05-11
FI932552A0 (en) 1993-06-04
HU9301672D0 (en) 1993-09-28
GR3018685T3 (en) 1996-04-30

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